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CAR-T QA C&Q Engineer

Life Sciences
Validation and Qualification
Location
Ghent, East Flanders
Work type
Consultancy
Work model
Fulltime, Hybrid

Our client, a leader in innovative pharmaceutical solutions, is seeking a CAR-T QA C&Q Engineer to join their specialized quality team. This role focuses on the review and approval of qualification activities for facilities, utilities, and process equipment within a cutting-edge manufacturing environment.

Responsibilities

  • Review and approve qualification and requalification documentation, including protocols, reports, and URS for facilities and process equipment.
  • Ensure the qualification status of critical production assets by identifying and controlling all system critical aspects related to process requirements.
  • Investigate equipment-related deviations and implement effective CAPA plans to ensure continuous compliance and quality.
  • Manage the compliance status of production assets through the review of calibration records, maintenance plans, and master data setup.
  • Oversee data integrity deliverables by reviewing system audit trails and performing user access reviews for critical assets.
  • Represent the QA qualification function as a technical expert during regulatory and customer inspections.
  • Contribute to process improvement and optimization projects to ensure alignment with international regulations and industry practices.

Requirements

  • You have a Master’s degree in Engineering, Pharmaceutical Sciences, or a related analytical field.
  • You bring knowledge of cGMP regulations and FDA/EU guidance related to pharmaceutical or cell therapy manufacturing.
  • You possess experience in qualification and validation processes including change control, URS, and IA.
  • You have affinity with computerized systems, including parameter configurations and data management in production environments.
  • You bring strong analytical thinking, risk assessment skills, and a collaborative, solution-oriented mindset.
  • You are fluent in Dutch and English.

Nice to Haves

  • Experience acting as a subject matter expert during health authority inspections.
  • Advanced knowledge of data integrity standards for production assets.

Offer

  • Enjoy a competitive salary package with extra perks that recognize your talent.
  • Advance your career with a clear growth path, coaching, and mentoring to support you.
  • Thrive in a dynamic and supportive environment where you can truly make an impact.
  • Work when and where you perform best, ensuring an optimal work-life balance.
  • Choose a flexible transport solution, from a company car to a public transport subscription.
  • Expand your network and enjoy unforgettable moments at exclusive events and afterworks.
  • Grow your skills with external courses and our in-house Pauwels Academy.
  • Work on exciting projects with industry leaders in Life Sciences, Engineering & Digital.
  • Seize opportunities at every level, from a strong start to career acceleration and expert collaboration.

Thank you for your interest. Unfortunately, job applications are not available in your region. To ensure a high-quality match for our clients and streamline the application process, we have certain regional limitations in place. We value all potential candidates and encourage you to explore opportunities with us in the future.

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